Evidence map›Paper›PMID 27437776›Full record

ArticleOncotarget2016

YAP and 14-3-3γ are involved in HS-OA-induced growth inhibition of hepatocellular carcinoma cells: A novel mechanism for hydrogen sulfide releasing oleanolic acid.

Guanglin Xu, Jing Wang, Fangfang Wu, Na Wang, Wenli Zhou, Qian Wang, Wang Pan, Guizhen Ao, Jiquan Yang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Therapeutic potential of oleanolic acid in liver diseases.Naunyn-Schmiedeberg's archives of pharmacology · 2024
    Review
  4. Review
  5. Article
  6. Review
  7. The Ambivalent Function of YAP in Apoptosis and Cancer.International journal of molecular sciences · 2018
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Guanglin XuCollege of Life Sciences, Nanjing Normal University, Nanjing, China.
Jing WangCollege of Life Sciences, Nanjing Normal University, Nanjing, China.
Fangfang WuCollege of Life Sciences, Nanjing Normal University, Nanjing, China.
Na WangCollege of Life Sciences, Nanjing Normal University, Nanjing, China.
Wenli ZhouCollege of Life Sciences, Nanjing Normal University, Nanjing, China.
Qian WangCollege of Life Sciences, Nanjing Normal University, Nanjing, China.
Wang PanCollege of Life Sciences, Nanjing Normal University, Nanjing, China.
Guizhen AoDepartment of Medicinal Chemistry, School of Pharmacy, Soochew University, Jiangsu, China.
Jiquan YangJiangsu Key Laboratory of 3D Printing Equipment and Manufacturing, Nanjing Normal University, Nanjing, China.
Nanjing Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hydrogen sulfide-releasing oleanolic acid (HS-OA) is an emerging novel class of compounds and consists of an oleanolic acid (OA) and a H2S-releasing moiety. Although it exhibits improved anti-inflammatory activity, its potency in human cancers has not been understood yet. In this study, we examined the effects of HS-OA on the growth of liver cancer cell lines and the underlying mechanisms.HS-OA inhibited the growth of all four cancer cell lines studied, with potencies of 10- to 30-fold greater than that of its counterpart (OA). HS-OA induced significant apoptosis and decreased viability, clonogenic activity and migration of Hep G2 cells. Further studies showed that HS-OA resulted in the reduction of YAP expression and its downstream targets, CTGF and CYR 61, thus promoting cell apoptosis. In addition, HS-OA caused a decrease of 14-3-3γ expression, which led to Bad translocation to the mitochondria, ΔΨm loss, cytochrome c release, caspase activation and a recovery of 14-3-3γ reversed these effects induced by HS-OA.These findings indicate that YAP and 14-3-3γ are involved in HS-OA's effects on liver cancer cells and identifying HS-OA as a potential new drug candidate for cancer therapy.

Indexed as

14-3-3 ProteinsAdaptor Proteins, Signal TransducingAntineoplastic AgentsCarcinoma, HepatocellularCell Line, TumorCell ProliferationHumansHydrogen SulfideLiver NeoplasmsOleanolic AcidPhosphoproteinsTranscription FactorsYAP-Signaling Proteins14-3-3 ProteinsAdaptor Proteins, Signal TransducingAntineoplastic AgentsHydrogen SulfideOleanolic AcidPhosphoproteinsTranscription FactorsYAP1 protein, humanYAP-Signaling Proteins14-3-3COX-2HCCHep G2YAP

Identifiers

PMID27437776
PMCPMC5239541
OpenAlexW2484697546

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.